6MLQ
Cryo-EM structure of microtubule-bound Kif7 in the ADP state
Summary for 6MLQ
Entry DOI | 10.2210/pdb6mlq/pdb |
EMDB information | 9140 |
Descriptor | Tubulin alpha-1A chain, Tubulin beta chain, Kinesin-like protein KIF7, ... (8 entities in total) |
Functional Keywords | microtubule tip-tracking, primary cilium, hedgehog signaling, motor protein |
Biological source | Homo sapiens (Human) More |
Total number of polymer chains | 3 |
Total formula weight | 145988.40 |
Authors | Mani, N.,Jiang, S.,Wilson-Kubalek, E.M.,Ku, P.,Milligan, R.A.,Subramanian, R. (deposition date: 2018-09-27, release date: 2019-05-01, Last modification date: 2024-03-13) |
Primary citation | Jiang, S.,Mani, N.,Wilson-Kubalek, E.M.,Ku, P.I.,Milligan, R.A.,Subramanian, R. Interplay between the Kinesin and Tubulin Mechanochemical Cycles Underlies Microtubule Tip Tracking by the Non-motile Ciliary Kinesin Kif7. Dev.Cell, 49:711-730.e8, 2019 Cited by PubMed Abstract: The correct localization of Hedgehog effectors to the tip of primary cilia is critical for proper signal transduction. The conserved non-motile kinesin Kif7 defines a "cilium-tip compartment" by localizing to the distal ends of axonemal microtubules. How Kif7 recognizes microtubule ends remains unknown. We find that Kif7 preferentially binds GTP-tubulin at microtubule ends over GDP-tubulin in the mature microtubule lattice, and ATP hydrolysis by Kif7 enhances this discrimination. Cryo-electron microscopy (cryo-EM) structures suggest that a rotated microtubule footprint and conformational changes in the ATP-binding pocket underlie Kif7's atypical microtubule-binding properties. Finally, Kif7 not only recognizes but also stabilizes a GTP-form of tubulin to promote its own microtubule-end localization. Thus, unlike the characteristic microtubule-regulated ATPase activity of kinesins, Kif7 modulates the tubulin mechanochemical cycle. We propose that the ubiquitous kinesin fold has been repurposed in Kif7 to facilitate organization of a spatially restricted platform for localization of Hedgehog effectors at the cilium tip. PubMed: 31031197DOI: 10.1016/j.devcel.2019.04.001 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (4.2 Å) |
Structure validation
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